Melatonin mitigates the lipopolysaccharide-induced myocardial injury in rats by blocking the p53/xCT pathway-mediated ferroptosis.

This article examined the therapeutic effect of melatonin (MT) on the lipopolysaccharide (LPS)-induced myocardial injury, and the mechanisms involved. Septic rat model was constructed by exposing to lipopolysaccharide (LPS), and treated by MT, Ferrostatin-1 (Fer-1) and Erastin (Era). Hematoxylin-eosin staining was executed to appraise myocardial injury. H9c2 cells that exposed to LPS to induce in vitro sepsis cell model were treated by MT. p53 overexpression vectors were transfected into H9c2 cells. Inflammation- and ferroptosis-related indicators were examined by enzyme-linked immunosorbent assay. Expression of p53, xCT and GPX4 was scrutinized by quantitative real-time polymerase chain reaction and Western blot. MT relieved myocardial injury in septic rats. It decreased IL-6 and TNF-α, elevated GPX4 and GSH, and reduced MDA and Fe2+ in myocardial tissues of septic rats. LPS induced p53 elevation and xCT reduction in rats' myocardial tissues. Nevertheless, MT treatment declined p53 and increased xCT in myocardial tissues of septic rats. Interestingly, the relieving effect of MT on myocardial injury in septic rats was enhanced by Fer-1, but reversed by Era. The LPS-induced H9c2 cell damage was relieved by MT treatment. Besides, MT decreased LDH, IL-6 and TNF-α, elevated xCT, GPX4 and GSH, and reduced MDA and Fe2+ in the LPS-induced H9c2 cells. Conversely, these influences of MT on the LPS-induced H9c2 cells were reversed by p53 overexpression. MT is proposed to be a promising agent for treating the LPS-induced myocardial injury, as it relieves myocardial injury by hindering the p53/xCT-mediated ferroptosis in the LPS-induced septic rats.

Research on the facile regeneration of degraded cathode materials from spent LiNi0.5Co0.2Mn0.3O2 lithium-ion batteries.

Rational reusing the waste materials in spent batteries play a key role in the sustainable development for the future lithium-ion batteries. In this work, we propose an effective and facile solid-state-calcination strategy for the recycling and regeneration of the cathode materials in spent LiNi0.5Co0.2Mn0.3O2 (NCM523) ternary lithium-ion batteries. By systemic physicochemical characterizations, the stoichiometry, phase purity and elemental composition of the regenerated material were deeply investigated. The electrochemical tests confirm that the material characteristics and performances got recovered after the regeneration process. The optimal material was proved to exhibit the excellent capacity with a discharge capacity of 147.9 mAh g-1 at 1 C and an outstanding capacity retention of 86% after 500 cycles at 1 C, which were comparable to those of commercial NCM materials.

Ni-Rh-based bimetallic conductive MOF as a high-performance electrocatalyst for the oxygen evolution reaction.

Metal-organic frameworks (MOFs) have recently been considered the promising catalysts due to their merits of abundant metal sites, versatile coordination groups, and tunable porous structure. However, low electronic conductivity of most MOFs obstructs their direct application in electrocatalysis. In this work, we fabricate an Ni-Rh bimetallic conductive MOF ([Ni2.85Rh0.15(HHTP)2]n/CC) grown in situ on carbon cloth. Abundant nanopores in the conductive MOFs expose additional catalytic active sites, and the advantageous 2D π-conjugated structure helps accelerate charge transfer. Owing to the introduction of Rh, [Ni2.85Rh0.15(HHTP)2]n/CC exhibited substantially improved oxygen evolution reaction (OER) activity and exhibited only an overpotential of 320 mV to achieve the current density of 20 mA cm-2. The remarkable OER performance confirmed by the electrochemical tests could be ascribed to the synergistic effect caused by the doped Rh together with Ni in [Ni2.85Rh0.15(HHTP)2]n/CC, thereby exhibiting outstanding electrocatalytic performance.

Structural and electrochemical progress of O3-type layered oxide cathodes for Na-ion batteries.

Sodium-ion batteries (SIBs) have attracted great attention being the most promising sustainable energy technology owing to their competitive energy density, great safety and considerable low-cost merits. Nevertheless, the commercialization process of SIBs is still sluggish because of the difficulty in developing high-performance battery materials, especially the cathode materials. The discovery of layered transition metal oxides as the cathode materials of SIBs brings infinite possibilities for practical battery production. Thereinto, the O3-type layered transition metal oxides exhibit attractive advantages in terms of energy density benefiting from their higher sodium content compared to other kinds of layered transition metal oxides. Enormous research studies have largely put forward their progress and explored a wide range of performance improvement approaches from the morphology, coating, doping, phase structure and redox aspects. However, the progress is scattered and has not logically evolved, which is not beneficial for the further development of more advanced cathode materials. Therefore, our work aims to comprehensively review, classify and highlight the most recent advances in O3-type layered transition metal oxides for SIBs, so as to scientifically cognize their progress and remaining challenges and provide reasonable improvement ideas and routes for next-generation high-performance cathode materials.

Direct regeneration of waste LiFePO4 cathode materials with a solid-phase method promoted by activated CNTs.

Annually increasing electric vehicles will undoubtedly end in tremendous amount of waste LiFePO4 (LFP) batteries. In this work, a highly-efficient and easy-going solid-phase method is proposed for direct regeneration of the waste LFP cathode material (W-LFP). The W-LFP is successfully regenerated via heat treatment with the addition of Li2CO3, CNTs and glucose. After activation, the dispersibility of CNTs in water is improved, making it easier to mix well with other materials. Also, the hydroxyl and carboxyl groups on CNTs have a certain degree of reducibility, which is conducive to the reduction of Fe3+ to Fe2+. After subsequent heat treatment, the three-dimensional conductive network composed of CNTs greatly enhances the conductivity and the ionic diffusion coefficient of LFP, thereby improving its electrochemical performance. Meanwhile, the decay and regeneration mechanisms of LFP are investigated by characterization and electrochemical testing. The regenerated LFP achieves an excellent specific capacity of 155.47 mAh/g at 0.05 C, which is around 99% that of new LFP. Additionally, the costs of main consumption in the regeneration process only account for 33.7% the price of new LFP. This low-cost, high-value-added and solid-phase direct regeneration process is proved to have great economic and energy-saving potential, which is promising for recycling the waste LFP cathode materials.

Research Advances in Amorphous-Crystalline Heterostructures Toward Efficient Electrochemical Applications.

Interface engineering of heterostructures has proven a promising strategy to effectively modulate their physicochemical properties and further improve the electrochemical performance for various applications. In this context related research of the newly proposed amorphous-crystalline heterostructures have lately surged since they combine the superior advantages of amorphous- and crystalline-phase structures, showing unusual atomic arrangements in heterointerfaces. Nonetheless, there has been much less efforts in systematic analysis and summary of the amorphous-crystalline heterostructures to examine their complicated interfacial interactions and elusory active sites. The critical structure-activity correlation and electrocatalytic mechanism remain rather elusive. In this review, the recent advances of amorphous-crystalline heterostructures in electrochemical energy conversion and storage fields are amply discussed and presented, along with remarks on the challenges and perspectives. Initially, the fundamental characteristics of amorphous-crystalline heterostructures are introduced to provide scientific viewpoints for structural understanding. Subsequently, the superiorities and current achievements of amorphous-crystalline heterostructures as highly efficient electrocatalysts/electrodes for hydrogen evolution reaction, oxygen evolution reaction, supercapacitor, lithium-ion battery, and lithium-sulfur battery applications are elaborated. At the end of this review, future outlooks and opportunities on amorphous-crystalline heterostructures are also put forward to promote their further development and application in the field of clean energy.

Metal-Organic Frameworks for Electrocatalytic Sensing of Hydrogen Peroxide.

The electrochemical detection of hydrogen peroxide (H2O2) has become more and more important in industrial production, daily life, biological process, green energy chemistry, and other fields (especially for the detection of low concentration of H2O2). Metal organic frameworks (MOFs) are promising candidates to replace the established H2O2 sensors based on precious metals or enzymes. This review summarizes recent advances in MOF-based H2O2 electrochemical sensors, including conductive MOFs, MOFs with chemical modifications, MOFs-composites, and MOF derivatives. Finally, the challenges and prospects for the optimization and design of H2O2 electrochemical sensors with ultra-low detection limit and long-life are presented.

MOF-derived CoNi,CoO,NiO@N-C bifunctional oxygen electrocatalysts for liquid and all-solid-state Zn-air batteries.

Metal-organic framework (MOF)-derived carbon composites with embedded metal alloy/metal oxides have attracted much attention due to their low-cost and excellent electrochemical reactivity. However, the drawback of this concept is the severe carbon evaporation during their synthesis, resulting in a reduction of active sites and catalytic durability. To solve this problem, this study proposes the possibility of using Ketjen black (KB) to replenish the carbon content. Impressively, MOF-derived bimetal and oxide N-doped porous carbon (CoNi-CoO-NiO@NC-800) exhibits extremely high catalytic activity with an oxygen reduction reaction (half-wave potential: 0.83 V) and oxygen evolution reaction (overpotential: 352 mV @ 10 mA cm-2) potential gap of 0.75 V due to the virtue of the hierarchically porous structure and sufficient active sites. By combining theoretical studies, a strong synergetic coupling of the CoNi dual metal is proposed in decreasing the overall reaction barriers and promoting the reversible oxygen reactions. Moreover, the assembled liquid- and all-solid-state Zn-air batteries (ZABs) with the bifunctional catalyst as the air cathode demonstrate superior discharging (223 mW cm-2 at 310 mA cm-2) and charging-discharging performance and long lifetime (450 cycles, 75 h). This work will provide guidance for the rational design of metal/carbon hybrid catalysts and cut-price reproducible energy systems.

Rh particles in N-doped porous carbon materials derived from ZIF-8 as an efficient bifunctional electrocatalyst for the ORR and HER.

Durable and efficient electrocatalysts toward the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) are crucial to the development of sustainable energy conversion. In this article, we report a highly active bifunctional electrocatalyst derived from ZIF-8 through simple heat-treatment activation. The resultant catalyst is enriched with Rh nanoparticles in the carbon matrix, showing excellent ORR performance with a half-wave potential (E 1/2) of 0.803 V in alkaline electrolytes; it is simultaneously active for catalyzing the HER with an overpotential of 89 mV to reach a current density of 10 mA cm2 in acidic electrolytes. The prepared RhNC-900 catalyst (1.47 wt% Rh) is comparable to the commercial Pt/C catalyst (20 wt% Pt) in terms of the ORR in alkaline media and might inspire new ideas for the development of fuel cells and water splitting.

Conductive MOFs as bifunctional oxygen electrocatalysts for all-solid-state Zn-air batteries.

A new class of π-conjugated conductive metal-organic frameworks (MOFs) were developed as efficient electrocatalysts for both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Particularly when used as the bifunctional catalysts of an air-cathode, the conductive MOFs can help the all-solid-state Zn-air batteries to achieve a high performance.

2D Metal-Organic Frameworks (MOFs) for High-Performance BatCap Hybrid Devices.

Two identical layered metal-organic frameworks (MOFs) (CoFRS and NiFRS) are constructed by using flexible 1,10-bis(1,2,4-triazol-1-yl)decane as pillars and 1,4-benzenedicarboxylic acid as rigid linkers. The single-crystal structure analysis indicates that the as-synthesized MOFs possess fluctuant 2D networks with large interlayer lattices. Serving as active electrode elements in supercapacitors, both MOFs deliver excellent rate capabilities, high capacities, and longstanding endurances. Moreover, the new intermediates in two electrodes before and after long-lifespan cycling are also examined, which cannot be identified as metal hydroxides in the peer reports. After assembled into battery-supercapacitor (BatCap) hybrid devices, the NiFRS//activated carbon (AC) device displays better electrochemical results in terms of gravimetric capacitance and cycling performance than CoFRS//AC devices, and a higher energy-density value of 28.7 Wh kg-1 compared to other peer references with MOFs-based electrodes. Furthermore, the possible factors to support the distinct performances are discussed and analyzed.

Strontium Chloride-Passivated Perovskite Thin Films for Efficient Solar Cells with Power Conversion Efficiency over 21% and Superior Stability.

Industrialization of perovskite solar cells is constrained by adverse stability in the air. Herein, we report effective strontium chloride (SrCl2) passivation upon HC(NH2)2-CH3NH3 (FA-MA)-based perovskite thin films for the suppression of nonradiative recombination. Moreover, the recombination dynamics, crystallinity, carrier transport, morphology, and the elemental stoichiometry of this film were systematically studied. By optimizing the concentration of SrCl2, the corresponding devices exhibited an increased open-circuit voltage (1.00 V vs 1.09 V), consistent with the enhanced photoluminescence lifetime. The champion passivated device showed an ascendant power conversion efficiency (PCE) about 21.11%, with over 90% retention of the primal PCE in dry air after 1000 h of aging with 20-30% humidity. A superior stability and an accelerated electron/hole-extraction ability were further observed by time-resolved photoluminescence spectroscopy.

3-Layer conductive metal-organic nanosheets as electrocatalysts to enable an ultralow detection limit of H2O2.

Hydrogen peroxide has been widely studied in cell biology and liquid fuel cells as an oxidant or fuel, and highly efficient and durable electrocatalysts for H2O2 reduction and detection are in high demand. Here, a simple strategy to fabricate conductive 2D single/several-layer [Co3(HHTP)2]n MOF nanosheets, based on 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) and Co2+ ions, was developed by the Langmuir-Blodgett (LB) method combined with layer-by-layer (LbL) growth technology. The [Co3(HHTP)2]n MOF nanosheets successfully boosted H2O2 reduction with ultrahigh mass activity and good durability, and a new method to detect the H2O2 concentration with an ultralow detection limit of 10-7 (2.9 µmol L-1) was developed. Meanwhile, a series of factors like layer number, surface tension, pH value, ion concentration, and annealing were systematically investigated to further prove the ultrahigh accuracy, sensitivity, and durability of the as-developed H2O2 detection method. The reaction mechanism and energy transfer process of H2O2 reduction catalyzed by the metal-organic nanosheets were investigated by first principles calculations using density functional theory (DFT), showing good agreement with the experiment.

Efficient air-stable perovskite solar cells with a (FAI)0.46(MAI)0.40(MABr)0.14(PbI2)0.86(PbBr2)0.14 active layer fabricated via a vacuum flash-assisted method under RH > 50.

In this work, we present a new kind of perovskite, (FAI)0.46(MAI)0.40(MABr)0.14(PbI2)0.86(PbBr2)0.14, the vacuum flash-assisted solution processing (VASP) of which can be carried out under relative humidity (RH) higher than 50% in ambient air. The smooth and highly crystalline perovskite showed a maximum PCE of 18.8% in perovskite solar cells. This kind of perovskite was demonstrated to be of good stability in ambient air. Holes and electrons have larger and more balanced diffusion lengths (643.7/621.9 nm) than those in the MAPbI3 perovskite (105.0/129.0 nm) according to the PL quenching experiment. The role of incorporating a large amount of MA+ cations to stabilize the intermediate phase via VASP under high RH is attributed to their better ability to intercalate into the sharing face of the one-dimensional face-sharing [PbI6] octahedra, forming the three-dimensional corner-sharing form. Moreover, hole/electron transfer times at the perovskite/Spiro-OMeTAD (PCBM) interfaces (8.90/9.20 ns) were found to be much larger than those in the MAPbI3 perovskite (0.75/0.40 ns), indicating that there still is enormous potential in further improving the performance of this kind of perovskite solar cell by interfacial engineering.

Fewer-layer conductive metal-organic nanosheets enable ultrahigh mass activity for the oxygen evolution reaction.

A new class of 2D fewer-layer π-conjugated conductive metal-organic nanosheets was developed via the Langmuir-Blodgett method, exhibiting ultrahigh mass activity (64.63 A mg-1, 1.7 V vs. RHE) and stability for electrochemical oxygen evolution reactions (OER).

Effects of Risperidone and Paliperidone on Brain-Derived Neurotrophic Factor and N400 in First-Episode Schizophrenia.

BACKGROUND: Risperidone and paliperidone have been the mainstay treatment for schizophrenia and their potential role in neuroprotection could be associated with brain-derived neurotrophic factor (BDNF) and N400 (an event-related brain potential component). So far, different effects on both BDNF and N400 were reported in relation to various antipsychotic treatments. However, few studies have been conducted on the mechanism of risperidone and paliperidone on BDNF and N400. This study aimed to compare the effects of risperidone and paliperidone on BDNF and the N400 component of the event-related brain potential in patients with first-episode schizophrenia. METHODS: Ninety-eight patients with first-episode schizophrenia were randomly divided into the risperidone and paliperidone groups and treated with risperidone and paliperidone, respectively, for 12 weeks. Serum BDNF level, the latency, and amplitude of the N400 event-related potential before and after the treatment and Positive and Negative Syndrome Scale (PANSS) scores were compared between the two groups. RESULTS: A total of 94 patients were included in the final analysis (47 patients in each group). After the treatment, the serum BDNF levels in both groups increased (all P < 0.01), while no significant difference in serum BDNF level was found between the groups before and after the treatment (all P > 0.05). After the treatment, N400 amplitudes were increased (from 4.73 ± 2.86 µv and 4.51 ± 4.63 µv to 5.35 ± 4.18 µv and 5.52 ± 3.08 µv, respectively) under congruent condition in both risperidone and paliperidone groups (all P < 0.01). Under incongruent conditions, the N400 latencies were shortened in the paliperidone group (from 424.13 ± 110.42 ms to 4.7.41 ± 154.59 ms, P < 0.05), and the N400 amplitudes were increased in the risperidone group (from 5.80 ± 3.50 µv to 7.17 ± 5.51 µv, P < 0.01). After treatment, the total PANSS score in both groups decreased significantly (all P < 0.01), but the difference between the groups was not significant (P > 0.05). A negative correlation between the reduction rate of the PANSS score and the increase in serum BDNF level after the treatment was found in the paliperidone group but not in the risperidone group. CONCLUSIONS: Both risperidone and paliperidone could increase the serum BDNF levels in patients with first-episode schizophrenia and improve their cognitive function (N400 latency and amplitude), but their antipsychotic mechanisms might differ.

Novel MOF-Derived Co@N-C Bifunctional Catalysts for Highly Efficient Zn-Air Batteries and Water Splitting.

Metal-organic frameworks (MOFs) and MOF-derived materials have recently attracted considerable interest as alternatives to noble-metal electrocatalysts. Herein, the rational design and synthesis of a new class of Co@N-C materials (C-MOF-C2-T) from a pair of enantiotopic chiral 3D MOFs by pyrolysis at temperature T is reported. The newly developed C-MOF-C2-900 with a unique 3D hierarchical rodlike structure, consisting of homogeneously distributed cobalt nanoparticles encapsulated by partially graphitized N-doped carbon rings along the rod length, exhibits higher electrocatalytic activities for oxygen reduction and oxygen evolution reactions (ORR and OER) than that of commercial Pt/C and RuO2 , respectively. Primary Zn-air batteries based on C-MOF-900 for the oxygen reduction reaction (ORR) operated at a discharge potential of 1.30 V with a specific capacity of 741 mA h gZn-1 under 10 mA cm-2 . Rechargeable Zn-air batteries based on C-MOF-C2-900 as an ORR and OER bifunctional catalyst exhibit initial charge and discharge potentials at 1.81 and 1.28 V (2 mA cm-2 ), along with an excellent cycling stability with no increase in polarization even after 120 h - outperform their counterparts based on noble-metal-based air electrodes. The resultant rechargeable Zn-air batteries are used to efficiently power electrochemical water-splitting systems, demonstrating promising potential as integrated green energy systems for practical applications.

Effects of Repetitive Transcranial Magnetic Stimulation Treatment on Event-Related Potentials in Schizophrenia.

BACKGROUND: Repetitive transcranial magnetic stimulation (rTMS) and event-related potentials (ERPs) are a noninvasive technique that widely used in neurophysiological field. Although rTMS has shown clinical utility for a number of neurological conditions, Recently,there was little understanding of the the efficacy of rTMS on Schizophrenia(SZ) and the change of ERP between before and after rTMS treatment. The objective of this study was to investigate the characteristics of N400, mismatch negativity (MMN), and P300 before and after treatment with rTMS in SZ. METHODS: One hundred and twenty-seven SZ patients hospitalized in Shanghai Mental Health Center from March 2015 to July 2017, divided into two groups (85 patients were recruited as rTMS group and 42 were recruited as sham rTMS [ShrTMS] group) and 76 normal controls (NCs) who were the staff and refresher staff in our hospital were recruited at the same time. A Chinese-made rTMS and a Runjie WJ-1 ERPs instrument were used in the present experiment. N400 was elicited by congruent and noncongruent Chinese idioms. After rTMS treatment, N400, P300, and MMN characteristics were compared with those before treatment and NC group. RESULTS: Compared with NC, the SZ patients exhibited delays in N400, P300, and MMN latency and decreased N400, P300, and MMN amplitudes in their frontal area (P < 0.05). After 25 rTMS treatments, N400 amplitudes in the frontal area (elicited by idioms with same phonic and different shape and meaning and with different phonic, shape, and meaning) were increased in the SZ patients (P < 0.05). However, there was no significant change in N400 before and after treatment with ShrTMS in SZ patients (P > 0.05). Amplitudes for MMN and target P300 also increased in SZ patients after rTMS treatment (P < 0.05). CONCLUSIONS: Based on our preliminary findings, we believe that the combined usage of N400, MMN, and P300 could be a valuable index and an electrophysiological reference in evaluating the effects of rTMS treatment in SZ patients.

3D hole-transporting materials based on coplanar quinolizino acridine for highly efficient perovskite solar cells.

Over the past five years, perovskite solar cells (PSCs) have gained intense worldwide attention in the photovoltaic community due to their low cost and high power conversion efficiencies (PCEs). One of the most significant issues in achieving high PCEs of PSCs is the development of suitable low-cost hole-transporting materials (HTMs). Here, we put forward a new concept of HTMs for PSCs: a 3D structure with a core of coplanar quinolizino acridine, derived from the conventional concept of 2D triphenylamine HTMs. A cheaper Ag nanolayer was utilized to replace Au as the counter electrodes, and the title HTM TDT-OMeTAD was synthesized via an easy four-step synthesis (total yield: 61%) to achieve the low cost and convenient manufacture of PSCs. Compared with the conventional 2D triphenylamine HTM, TTPA-OMeTPA, PSC devices based on the 3D HTM TDT-OMeTPA showed a significant improvement in PCE from 10.8% to 16.4%, even outperforming Spiro-OMeTAD (14.8%). TDT-OMeTAD's highest PCE mainly results from it having the highest open-circuit voltage (Voc) of 1.01 V in this work, which is proven to be due to the higher hole mobility, matching energy levels, higher hydrophobicity and the smaller dark current. Moreover, an incident photon-current conversion efficiency (IPCE) test and time-resolved photoluminescence (TRPL) have been carried out to observe the better hole injecting efficiency and photoelectric conversion capability of TDT-OMeTPA based PSCs than Spiro-OMeTAD. The TDT-OMeTPA based PSCs exhibited >75% reproducibility (PCE > 15%) and retained 93.2% of the initial PCE after >500 hours.

A pair of 3D enantiotopic zinc(ii) complexes based on two asymmetric achiral ligands.

Enantiomorphism and enantioselectivity are critical in biology and many other applications. Herein, we report two 3D chiral MOFs {[Zn6(MIDPPA)3(1,2,4-btc)3(NO2)3(H2O)3](H2O)7}n (1L and 1R) based on achiral ligands with high enantiomeric excess and a novel topological type. The internal mechanism of spontaneous chiral symmetry breaking, during the crystallization of chiral MOFs based on achiral ligands, is elucidated for the first time from both structural and theoretical aspects. Hydrogen bonds are found to play a key role in the spontaneous symmetry breaking of chiral MOFs. Also, DFT calculations support our findings from the aspects of total energies and HOMO-LUMO energy gaps. Both 1L and 1R, exhibiting green fluorescence, present a non-centrosymmetric polar packing arrangement, resulting in good ferroelectric behaviors and second-order nonlinear optical effects.